Evidence map›Paper›PMID 34612064›Full record

ReviewAmerican journal of physiology. Lung cellular and molecular physiology2021

Human microphysiological models of airway and alveolar epithelia.

Dave Anuj Lagowala, Seoyoung Kwon, Venkataramana K Sidhaye, Deok-Ho Kim

Abstract readReview
In one paragraph

Review in American journal of physiology. Lung cellular and molecular physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Review
  2. Endothelial Continuum and Capillary Specialization in Pulmonary Vascular Development.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Microphysiological systems to advance human pathophysiology and translational medicine.Journal of applied physiology (Bethesda, Md. : 1985) · 2024
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Engineering and Modeling the Lung Mesenchyme.Advances in experimental medicine and biology · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Dave Anuj LagowalaDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland.
Seoyoung KwonDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland.
Venkataramana K SidhayeDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.ORCID 0000-0002-4506-8549
Deok-Ho KimDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland.ORCID 0000-0002-6989-6074

Funding

Modeling of human HSV infection: development of immune-competent 3D skin-on-chip with vascular perfusionR01AI143773 · NIAID · UNIVERSITY OF WASHINGTON · PI ZHU, JIA · 2020 to 2024
$2.7M
Role of E-cadherin in modulating airway epithelial function and parenchymal remodelingR01HL151107 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SIDHAYE, VENKATARAMANA K · 2020 to 2023
$2.4M
Actin-myosin contractility promotes the development of chronic bronchitisR01HL124099 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SIDHAYE, VENKATARAMANA K · 2017 to 2021
$2.1M
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL124099HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL151107HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R01AI143773Korea Health Industry Development Institute (KHIDI) HI19C0642NHLBI NIH HHS R01 HL124099NHLBI NIH HHS R01 HL151107NIAID NIH HHS R01 AI143773
6 · The paper itself

Abstract

Human organ-on-a-chip models are powerful tools for preclinical research that can be used to study the mechanisms of disease and evaluate new targets for therapeutic intervention. Lung-on-a-chip models have been one of the most well-characterized designs in this field and can be altered to evaluate various types of respiratory disease and to assess treatment candidates prior to clinical testing. These systems are capable of overcoming the flaws of conventional two-dimensional (2-D) cell culture and in vivo animal testing due to their ability to accurately recapitulate the in vivo microenvironment of human tissue with tunable material properties, microfluidic integration, delivery of precise mechanical and biochemical cues, and designs with organ-specific architecture. In this review, we first describe an overview of currently available lung-on-a-chip designs. We then present how recent innovations in human stem cell biology, tissue engineering, and microfabrication can be used to create more predictive human lung-on-a-chip models for studying respiratory disease. Finally, we discuss the current challenges and future directions of lung-on-a-chip designs for in vitro disease modeling with a particular focus on immune and multiorgan interactions.

Indexed as

Models, BiologicalAlveolar Epithelial CellsAnimalsDrug Evaluation, PreclinicalHumansLab-On-A-Chip DevicesRespiratory MucosaRespiratory Tract DiseasesTissue Engineering3-D culturelung-on-a-chipmicrofluidicsorgan-on-a-chiprespiratory system

Identifiers

PMID34612064
PMCPMC8715018

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.